Understanding (1-Boc-5,6-dichloro-1H-indol-2-yl)boronic Acid: A Chemical Synthesis Essential
In the specialized realm of chemical synthesis, certain compounds emerge as linchpins for innovation. (1-(tert-Butoxycarbonyl)-5,6-dichloro-1H-indol-2-yl)boronic acid, identified by its CAS number 1310384-28-1, is such a compound, proving essential for researchers and manufacturers alike. This article delves into the technical aspects of this intermediate and provides guidance for those looking to buy it, emphasizing the value of sourcing from reputable manufacturers and suppliers, particularly within China.
Technical Insights into the Intermediate
(1-(tert-Butoxycarbonyl)-5,6-dichloro-1H-indol-2-yl)boronic acid is a complex organic molecule featuring a functionalized indole ring. The presence of the tert-butoxycarbonyl (Boc) group serves as a protective measure for the indole nitrogen atom, crucial for controlling reactivity during multi-step synthesis. The boronic acid moiety (-B(OH)2) is a highly versatile functional group, renowned for its participation in palladium-catalyzed cross-coupling reactions, such as the Suzuki-Miyaura reaction. These reactions are fundamental in modern synthetic chemistry, enabling the formation of carbon-carbon bonds with high efficiency and selectivity. This makes the compound invaluable for building complex molecular structures, often found in pharmaceutical intermediates, agrochemicals, and advanced materials. A typical specification for this compound is a purity of 97% or higher, ensuring its suitability for demanding synthetic procedures where side products must be minimized. Its molecular formula is C13H14BCl2NO4, with a molecular weight of 329.972.
Procurement: Where to Buy and Why
For professionals seeking to purchase (1-(tert-Butoxycarbonyl)-5,6-dichloro-1H-indol-2-yl)boronic acid, identifying reliable sources is key. China has become a major global player in chemical manufacturing, offering a broad spectrum of intermediates at competitive prices. When choosing a supplier or manufacturer, it is important to verify their credentials, quality control processes, and ability to provide consistent supply. A reputable China-based company will offer detailed product specifications, including the CAS number, purity, and safety data. They are typically willing to provide a free sample, which is an excellent way to confirm the quality before committing to a larger order. Direct engagement with a manufacturer also often allows for better negotiation on price and potential for custom packaging or synthesis requirements. Our company, as a dedicated chemical provider, focuses on delivering high-quality intermediates like this to the global research community.
Applications and Strategic Value
The strategic value of (1-(tert-Butoxycarbonyl)-5,6-dichloro-1H-indol-2-yl)boronic acid is most evident in the pharmaceutical industry, where it serves as a building block for active pharmaceutical ingredients (APIs) and drug candidates. Its ability to facilitate complex bond formations makes it a preferred reagent for medicinal chemists designing new molecules. The compound's utility also extends to academic research and the development of new functional materials. By partnering with a reliable manufacturer from China, you can ensure access to this essential intermediate, streamlining your research and development efforts and potentially reducing costs. We invite you to contact us to discuss your requirements and obtain a quote for this critical chemical synthesis essential.
Perspectives & Insights
Silicon Analyst 88
“This article delves into the technical aspects of this intermediate and provides guidance for those looking to buy it, emphasizing the value of sourcing from reputable manufacturers and suppliers, particularly within China.”
Quantum Seeker Pro
“Technical Insights into the Intermediate (1-(tert-Butoxycarbonyl)-5,6-dichloro-1H-indol-2-yl)boronic acid is a complex organic molecule featuring a functionalized indole ring.”
Bio Reader 7
“The presence of the tert-butoxycarbonyl (Boc) group serves as a protective measure for the indole nitrogen atom, crucial for controlling reactivity during multi-step synthesis.”